Does AMLODIPINE\TELMISARTAN Cause Product dose omission? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product dose omission have been filed in association with AMLODIPINE\TELMISARTAN. This represents 3.3% of all adverse event reports for AMLODIPINE\TELMISARTAN.
16
Reports of Product dose omission with AMLODIPINE\TELMISARTAN
3.3%
of all AMLODIPINE\TELMISARTAN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission From AMLODIPINE\TELMISARTAN?
Of the 16 reports.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMLODIPINE\TELMISARTAN. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does AMLODIPINE\TELMISARTAN Cause?
Hypotension (70)
Toxicity to various agents (66)
Balance disorder (60)
Depressed level of consciousness (60)
Pain (60)
Constipation (59)
Blood calcium decreased (57)
Fall (57)
Sedation complication (56)
Cognitive disorder (55)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which AMLODIPINE\TELMISARTAN Alternatives Have Lower Product dose omission Risk?
AMLODIPINE\TELMISARTAN vs AMLODIPINE\VALSARTAN
AMLODIPINE\TELMISARTAN vs AMMONIUM
AMLODIPINE\TELMISARTAN vs AMNESTEEM
AMLODIPINE\TELMISARTAN vs AMOXAPINE
AMLODIPINE\TELMISARTAN vs AMOXICILLIN